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REVIEW 3 major objections 4 minor 90 references

Compositional Covariate Importance Testing via Partial Conjunction of Bivariate Hypotheses

T0 review · 3 major / 4 minor · reviewed 2026-08-10 · deepseek-v4-flash

Pith's one-line read Compositional covariates defeat standard importance tests; this paper defines importance as the unique nontrivial Markov boundary and tests it via partial conjunction of bivariate conditional hypotheses.

desk verdict Novel and valuable theory for compositional covariate importance, but the power-advantaged methods rely on an unproven PRDS assumption and two appendix proofs need fixing. read the letter →

arxiv 2501.00566 v1 pith:BPGHAICO submitted 2024-12-31 stat.ME math.STstat.TH

classification stat.MEmath.STstat.TH MSC 62H1562G10
keywords compositionaldataMarkovboundarybivariateconditionalindependencepartialconjunctionhypothesismultipletestingfalsediscoveryratefamilywiseerrorrandomizationtest
verification ladder T0 review T1 audit T2 compute T3 formal

The pith

A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.

The reading

Compositional covariates arise whenever a total is split into parts, such as microbiome relative abundances, time-use budgets, or voting shares, and they silently break standard regression tools: each covariate is a deterministic function of the others, so every conditional importance test is trivially true and every marginal test is trivially false. This paper establishes that a workable notion of importance still exists: under mild conditions, the unique nontrivial Markov boundary of the response exists and equals the set $S$ of covariates $j$ for which every bivariate conditional hypothesis $Y \perp\!\!\perp X_{i,j} \mid X_{i,j}^c$ (for all $i \neq j$) is false. It then shows that testing membership in $S$ reduces to a partial conjunction hypothesis test, and builds single-test and multiple-testing procedures called BCP with proven FWER and FDR control. Simulations indicate the methods are valid and powerful across Dirichlet, logistic-normal, sparse-compositional, and even non-compositional covariate distributions.

What carries the argument

The load-bearing object is the bivariate conditional independence hypothesis $H_{i,j}: Y \perp\!\!\perp X_{i,j} \mid X_{i,j}^c$, which is non-degenerate under compositionality because conditioning on all but two coordinates leaves a random pair. The set $S$ aggregates these hypotheses, and Theorem 2.1 connects $S$ to the Markov boundary via an iterated set operation $(\Delta \circ)^k I$ built from an intersection-property lemma for supports with a single equivalence class. On the testing side, the paper's methods are partial conjunction hypothesis (PCH) tests — hypotheses stating that fewer than $r$ of a collection of base hypotheses are false — applied to the bivariate p-values, combined with Bonferroni or Simes global tests, and then wrapped in Holm-style or Benjamini-Hochberg multiple testing procedures to form the BCP family. This machinery converts an untestable definition (a Markov boundary on a measure-zero support) into a testable composite of ordinary conditional independence tests.

What would settle it

Generate compositional covariates with a known sparse Markov boundary (e.g., $Y = X_1 + \varepsilon$, $X$ Dirichlet) but force the bivariate p-values to be negatively dependent — for instance by using antithetic resampling in the conditional randomization test — and apply BCP($\bar{s}$)-BH at FDR 10%. If the empirical FDR exceeds 10%, Theorem 3.3's Simes-based guarantee is refuted. Alternatively, a distribution like Example 2 where the path-connectivity condition of Corollary 2.1 fails should produce multiple nontrivial Markov boundaries, checking the uniqueness claim.

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Extended reading notes

Core claim

The paper's central theoretical result is Theorem 2.1: for compositional $X$, if $S=[p]$ then no nontrivial Markov boundary exists, and otherwise, provided $S^c \in (\Delta \circ)^k I$ for some $k$, $S$ is the unique nontrivial Markov boundary, where $H_{i,j}: Y \perp\!\!\perp X_{i,j} \mid X_{i,j}^c$, $I=\{\{i,j\}: H_{i,j} \text{ true}\}$, and $\Delta$ collects pairs of sets for which an intersection-property lemma applies. Under Assumption 1, each hypothesis $H_{0j}: j\notin S$ equals a partial conjunction hypothesis: fewer than $r$ of the bivariate nulls for that $j$ are false, and any strict upper bound $\bar{s}>|S|$ yields a valid test. The paper proves validity of Bonferroni-based BCP tests under arbitrary dependence, and Simes-based BCP tests under a PRDS condition on the base p-values; it also proves FWER control for Holm-style BCP algorithms and FDR control for a Benjamini-Hochberg BCP algorithm.

Load-bearing premise

The Simes-based BCP methods, which carry the main power advantages and are used in the primary simulations, are valid only if the bivariate base p-values are positively regression dependent on each null subset (PRDS); the paper calls this plausible but not easily provable, and supplies no concrete conditional-independence test with a proven PRDS guarantee.

Editorial extensions

If this is right

  • Standard conditional-independence-based variable selection and testing, including parametric coefficient tests, knockoffs, and conditional randomization tests, has provably trivial power on compositional covariates; BCP methods restore nontrivial, error-controlled inference.
  • When an upper bound $\bar{s}$ on the number of important covariates is known (for example $\bar{s}=p/2$), BCP tests are substantially more powerful than the always-valid default $\bar{s}=p-1$.
  • The scope extends beyond compositional vectors: the same theory and procedures apply to covariates satisfying any single deterministic constraint, including linear subspaces or the unit sphere.
  • Conditioning on covariates that are a priori sparse (Theorem 3.4) recovers power without sacrificing validity, as long as $|S^c \cap D| \neq 1$.
  • In non-compositional regression settings, BCP methods retain most of the power of state-of-the-art univariate conditional independence tests, so the same toolbox transfers without loss.

Reading between the lines

Editorial extensions of the paper, not claims the author makes directly.

  • The PRDS assumption could be verified for concrete conditional-independence tests: for instance, the distilled conditional randomization test with Gaussian designs may satisfy PRDS under exchangeable resampling, which would upgrade Corollary 3.2 and Theorem 3.3 from plausible to proven.
  • The same PCH-of-bivariate-hypotheses construction might extend to multiple deterministic constraints (e.g., $k$ constraints) by testing $k$-variate conditional independence, but at $O(p^{k+1})$ hypotheses; the paper's screening speedups suggest a possible path to tractability.
  • For experimental design, Remark 2 shows the Markov boundary can depend on the support of $X$, not just on $Y\mid X$; this implies that the choice of design partially determines the scientifically meaningful target of selection.
  • The paper's methods could be used as a diagnostic for whether a compositional regression problem has any parsimonious structure: if $S=[p]$ (all bivariate tests false), no nontrivial Markov boundary exists and all covariates are effectively important.
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Editorial analysis

A structured set of objections, weighed in public.

Desk editor's note, referee report, and a circularity audit.

Referee Report

3 major / 4 minor

Summary. The paper addresses covariate importance testing when covariates are compositional. Because each compositional covariate is a deterministic function of the others, standard conditional independence hypotheses are degenerate, and unconditional hypotheses are all false in typical sparse models. The authors define the set of important covariates via the Markov boundary, prove under conditions that it coincides with the set S of indices j for which every bivariate conditional independence hypothesis H_{i,j}: Y ⊥⊥ X_{i,j} | X_{i,j}^c is false, and then test membership in S through partial conjunction hypotheses built from bivariate p-values. They propose BCP procedures: Bonferroni-based tests valid under arbitrary dependence, and Simes-based tests and BH/Holm multiple testing procedures whose validity requires a PRDS assumption on the base p-values. Numerical experiments compare these methods with leave-one-out and univariate benchmarks in compositional, non-compositional, and sparse compositional settings.

Significance. If the results hold, this is a valuable contribution: it gives a principled, falsifiable definition of relevant compositional covariates and connects it to a practical testing framework. The Markov-boundary characterization in Theorem 2.1 and the Bonferroni-based error control results are rigorous under the stated assumptions, and the paper includes reproducible code and extensive simulations. The Janus-faced nature of conditional and unconditional hypotheses under compositionality is clearly explained. However, the power-oriented methods advertised and used throughout the main text rest on an unverified PRDS assumption, and two appendix proofs that support the main simplifying corollaries contain gaps. The significance is therefore high conditional on repair of these issues.

major comments (3)
  1. [Section 3.1, Corollary 3.2, Theorems 3.2 and 3.3] The Simes-based BCP procedures, which are the methods used in all main-text simulations and recommended for their power, are valid only if the base p-values are positively regression dependent on each null subset (PRDS). The manuscript itself says this is "plausible (if not easily provable)" and provides no conditional independence test, including the dCRT used in the simulations, for which PRDS is actually established. The dCRT p-values share the same response and overlapping conditioning sets, so their joint dependence is complex and not obviously PRDS. Moreover, Section 3.5's data-dependent screening changes the dependence structure, and the paper concedes it "could in principle impact the validity" of the positive-dependence-based procedures. Since the advertised power advantages and the FWER/FDR guarantees for BCP(s)-Holm and BCP(s)-BH rest on this unverified assumption, I request either a proven PRDS result for a concrete test class (e.g., the dCRT under the Gaussian or Dirichlet simulation models) or a restructuring that presents the Bonferroni-based procedures as the formally guaranteed methods and the Simes-based procedures as empirically supported heuristics.
  2. [Appendix B.3, proof of Corollary 2.1] The constructed point w† in Step 3 can fail to lie in the simplex, so the claimed equivalence proof is incomplete. In the first case, the coordinate of w† corresponding to A∩B is 1 - sum_{j in A\B} w_j - w*_{B\A} - sum c_j, and the displayed inequality does not prevent this coordinate from being negative. The subsequent claim f_X(w†) > 0 follows only if w† is in the relevant ball within the simplex slice, which is not established. This gap affects Corollary 2.1, the main simplification of Theorem 2.1 for continuous compositional distributions, and needs to be repaired before the corollary can be considered proven.
  3. [Appendix B.4, proof of Corollary 2.2] The proof of Corollary 2.2 for factor covariates has a serious gap. In Step 4, after applying Lemma 2.2 to A = S_F^c ∩ F_k and B = M^c ∩ F_k^c, the displayed conditioning set and the claimed blanket are not coherent: the set (S_F ∩ F_k) ∪ (M ∪ F_k^c) is not generally a subset of M, so it cannot contradict the minimality of the Markov boundary M. The derivation of Y ⊥⊥ X_{S_F^c ∩ F_k} | X_{(S_F ∩ F_k) ∪ F_k^c} also needs justification. As stated, Corollary 2.2 is not proven and should either be supplied with a corrected argument or explicitly deferred.
minor comments (4)
  1. [Figure 1 caption] The word "selelction" should be "selection".
  2. [Corollaries 2.1 and 2.2, assumption (i)] The condition "for all i, j in S^c" should require i ≠ j, since H_{i,i} is not defined. The same comment applies to Corollary 2.2 and Corollary C.1.
  3. [Appendix B.3, Step 2] The text "0 ≥ c < 1" appears to be a typo and should read "0 ≤ c < 1".
  4. [Section 3.1, Eq. (2) and (3)] The notation P_{(i),j} is used for order statistics of the p-values in column j, but the indexing in the displayed equations is not defined explicitly; a sentence defining P_{(i),j} as the ith smallest of {P_{i',j} : i' ≠ j} would improve readability.

Circularity Check

0 steps flagged · score 1.0 of 10

No significant circularity: the S/H_{i,j} connection is definitional but externally anchored by the Markov boundary; the main validity gap (unproven PRDS for Simes-based BCP) is an assumption, not a circular reduction.

full rationale

The derivation chain is self-contained. S is defined as {j: H_{i,j} false for all i≠j}, and H_{0j}: j∉S is exactly H^{p-1}_{0j}, a partial conjunction of the same bivariate CI hypotheses; this is a definitional identity used to build a test, not a prediction smuggled in. The external anchor is Theorem 2.1, proved in Appendix B.2 from Lemma 2.1 and Proposition B.1, showing S coincides with the unique nontrivial Markov boundary under the (Δ∘)^k I condition; the proof adapts Peters (2015), not self-citation. Corollaries 2.1/2.2/C.1 supply explicit sufficient conditions. The BCP validity results (Corollary 3.1, Theorems 3.1–3.3) follow from Benjamini–Heller/Bogomolov PCH theory applied to user-supplied valid base p-values; no parameter is fitted to data to manufacture a prediction. Self-citations (Ma et al. 2024, Liu et al. 2022) are used only for comparison or as an external test choice. The one caveat worth recording is that the Simes/BH procedures advertised for power require PRDS of the base p-values, which the paper explicitly labels 'plausible (if not easily provable)' (Section 3.1); if PRDS fails, those procedures may not control error rates. That is a substantive statistical assumption/limitation, but it is not a circular reduction of the paper's conclusions to its inputs. Data-dependent screening (Section 3.5) is similarly a caveat about dependence, not circularity. Overall: very low or no circularity burden; score 1 reflects only minor self-citation and definitional proximity, neither load-bearing.

Assumptions & free parameters 3 free parameters · 7 assumptions · 0 invented entities

The central claim rests on domain assumptions about compositional support, uniqueness of the Markov boundary (Assumption 1), validity of the base CI tests, and, for the recommended Simes procedures, PRDS of base p-values. User-chosen inputs such as the upper bound s and resample count are not fitted parameters. No new physical entities are introduced.

free parameters (3)
  • s (strict upper bound on |S|) = p-1, p/2, or s+1 in simulations
    User-specified input to BCP methods; smaller s gives more power but requires domain knowledge. Not fitted to data in the theory.
  • K (number of dCRT resamples) = 1500 (or 25,000 in one appendix)
    Monte Carlo resample count for base p-values; affects resolution of p-values, not a model parameter.
  • Screening p-value threshold for speedups = 0.1
    P-values above this are set to 1 to save computation; chosen by hand in Appendix E.9.
assumptions (7)
  • domain assumption X is compositional: sum_j X_j = 1 and X has no additional deterministic constraints beyond this (except the disjoint per-factor constraints in Section 2.3.2).
    Assumed throughout; Remark 1 notes that extra constraints would require trivariate or higher-order hypotheses.
  • domain assumption Assumption 1: either S = [p] and no nontrivial Markov boundary exists, or S is the unique nontrivial Markov boundary.
    Adopted in Section 3 before constructing tests; needed for the identity H_0j = H^{s+1}_{0j}.
  • domain assumption The bivariate conditional independence tests producing P_{i,j} are valid (super-uniform under H_{i,j}).
    Section 3.1 and 3.4 assume a valid CI test is available; dCRT in the simulations requires knowing or sampling the conditional distribution of X_{i,j}|X_{i,j}^c.
  • domain assumption For the Simes-based methods, the null base p-values are PRDS.
    Stated in Corollary 3.2, Theorem 3.2, Theorem 3.3; not proven for any concrete CI test, only empirically supported.
  • domain assumption The technical conditions of Corollary 2.1 (path-connectivity and graphical connection of true nulls) hold for continuous compositional distributions used in practice.
    Used to instantiate Theorem 2.1 for Dirichlet and logistic-normal covariates.
  • standard math The weak union and intersection properties of conditional independence, including the Peters (2015) version for non-Lebesgue supports, hold.
    Used in Lemma 2.1, Lemma 2.2, and several appendix proofs.
  • standard math Partial conjunction testing theory (Benjamini and Heller 2008) and the FDR result of Bogomolov (2021) apply as stated.
    The BCP p-values and FDR control argument are inherited from these results.

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Pith. "Pith review of Compositional Covariate Importance Testing via Partial Conjunction of Bivariate Hypotheses." pith.science (2026). https://pith.science/paper/BPGHAICO

@misc{pith2026250100566,
  author       = {Pith},
  title        = {Pith review of: Compositional Covariate Importance Testing via Partial Conjunction of Bivariate Hypotheses},
  year         = {2026},
  howpublished = {\url{https://pith.science/paper/BPGHAICO}},
  note         = {Machine review of arXiv:2501.00566}
}
read the original abstract

Compositional data (i.e., data comprising random variables that sum up to a constant) arises in many applications including microbiome studies, chemical ecology, political science, and experimental designs. Yet when compositional data serve as covariates in a regression, the sum constraint renders every covariate automatically conditionally independent of the response given the other covariates, since each covariate is a deterministic function of the others. Since essentially all covariate importance tests and variable selection methods, including parametric ones, are at their core testing conditional independence, they are all completely powerless on regression problems with compositional covariates. In fact, compositionality causes ambiguity in the very notion of relevant covariates. To address this problem, we identify a natural way to translate the typical notion of relevant covariates to the setting with compositional covariates and establish that it is intuitive, well-defined, and unique. We then develop corresponding hypothesis tests and controlled variable selection procedures via a novel connection with \emph{bivariate} conditional independence testing and partial conjunction hypothesis testing. Finally, we provide theoretical guarantees of the validity of our methods, and through numerical experiments demonstrate that our methods are not only valid but also powerful across a range of data-generating scenarios.

Figures

Figures reproduced from arXiv: 2501.00566 by the authors.

Figure 1
Figure 1. Comparison of methods for (a) single testing and (b) variable selelction with [PITH_FULL_IMAGE:figures/full_fig_p024_1.png] view at source ↗
Figure 2
Figure 2. Comparison of methods for (a) single testing and (b) multiple testing with [PITH_FULL_IMAGE:figures/full_fig_p026_2.png] view at source ↗
Figure 3
Figure 3. Effect of conditioning out the sparse covariates on power for single testing (left) [PITH_FULL_IMAGE:figures/full_fig_p027_3.png] view at source ↗
Figures from the paper (11 more)
Figure 4
Figure 4. Figure 4: Comparison of FWER and average power for variable selection with Dirichlet [PITH_FULL_IMAGE:figures/full_fig_p054_4.png]
Figure 5
Figure 5. Figure 5: Comparison of methods for (a) single testing, (b) FWER control and (c) FDR [PITH_FULL_IMAGE:figures/full_fig_p055_5.png]
Figure 6
Figure 6. Figure 6: Comparison of FWER and average power for variable selection with multivari [PITH_FULL_IMAGE:figures/full_fig_p056_6.png]
Figure 7
Figure 7. Figure 7: Effect of conditioning out the sparse covariates on type I error (left), FWER [PITH_FULL_IMAGE:figures/full_fig_p057_7.png]
Figure 8
Figure 8. Figure 8: Simulation studies showing the effects of sampling from an estimated Dirichlet [PITH_FULL_IMAGE:figures/full_fig_p058_8.png]
Figure 9
Figure 9. Figure 9: Comparison of BCP(s) with Simes and Bonferroni PC p-values. 61 [PITH_FULL_IMAGE:figures/full_fig_p061_9.png]
Figure 10
Figure 10. Figure 10: Comparison of BCP(s) with Simes and Bonferroni PC p-values for Logistic￾normal covariates. 62 [PITH_FULL_IMAGE:figures/full_fig_p062_10.png]
Figure 11
Figure 11. Figure 11: Comparison of BCP(s) with Simes and Bonferroni PC p-values for multivariate normal covariates. 63 [PITH_FULL_IMAGE:figures/full_fig_p063_11.png]
Figure 12
Figure 12. Figure 12: Comparison of effect of conditioning out sparse covariates on BCP( [PITH_FULL_IMAGE:figures/full_fig_p064_12.png]
Figure 13
Figure 13. Figure 13: Performance of AdaFilter on Dirichlet data in controlling (a) FWER and (b) [PITH_FULL_IMAGE:figures/full_fig_p065_13.png]
Figure 14
Figure 14. Figure 14: Comparison of proposed method with computational speedups discussed in [PITH_FULL_IMAGE:figures/full_fig_p066_14.png]

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Reference graph

Works this paper leans on

90 extracted references · 70 canonical work pages

  1. [1]

    Aitchison, J. (1982). The statistical analysis of compositional data. Journal of the Royal Statistical Society: Series B (Methodological) , 44(2):139--160

  2. [2]

    Barber, R. F. and Cand \`e s, E. J. (2015). Controlling the false discovery rate via knockoffs. Annals of Statistics

  3. [3]

    Baum, E. J. (1988). The use of pattern recognition to characterize air pollution regimes. Chemometrics and Intelligent Laboratory Systems , 3(1-2):91--98

  4. [4]

    and Heller, R

    Benjamini, Y. and Heller, R. (2008). Screening for partial conjunction hypotheses. Biometrics , 64(4):1215--1222

  5. [5]

    and Hochberg, Y

    Benjamini, Y. and Hochberg, Y. (1995). Controlling the false discovery rate: a practical and powerful approach to multiple testing. Journal of the Royal statistical society: series B (Methodological) , 57(1):289--300

  6. [6]

    and Yekutieli, D

    Benjamini, Y. and Yekutieli, D. (2001). The control of the false discovery rate in multiple testing under dependency. Annals of statistics , pages 1165--1188

  7. [7]

    Berger, J. O. and Pericchi, L. R. (1996). The intrinsic bayes factor for model selection and prediction. Journal of the American Statistical Association , 91(433):109--122

  8. [8]

    B., Wang, Y., Barber, R

    Berrett, T. B., Wang, Y., Barber, R. F., and Samworth, R. J. (2020). The conditional permutation test for independence while controlling for confounders. Journal of the Royal Statistical Society Series B: Statistical Methodology , 82(1):175--197

Show all 90 references
  1. [9]

    Bertsimas, D., King, A., and Mazumdar, R. (2016). Best subset selection via a modern optimization lens. The Annals of Statistics , 44(2):813--852

  2. [10]

    and Roquain, E

    Blanchard, G. and Roquain, E. (2008). Two simple sufficient conditions for fdr control

  3. [11]

    Bogomolov, M. (2021). Testing partial conjunction hypotheses under dependency, with applications to meta-analysis. arXiv preprint arXiv:2105.09032

  4. [12]

    and Heller, R

    Bogomolov, M. and Heller, R. (2018). Assessing replicability of findings across two studies of multiple features. Biometrika , 105(3):505--516

  5. [13]

    Box, G. E. and Hunter, J. S. (1957). Multi-factor experimental designs for exploring response surfaces. The Annals of Mathematical Statistics , pages 195--241

  6. [14]

    and Heethoff, M

    Br \"u ckner, A. and Heethoff, M. (2017). A chemo-ecologists’ practical guide to compositional data analysis. Chemoecology , 27:33--46

  7. [15]

    Buccianti, A., Mateu-Figueras, G., and Pawlowsky-Glahn, V. (2006). Compositional data analysis in the geosciences: from theory to practice , volume 264. Geological Society of London

  8. [16]

    Cand \`e s, E., Fan, Y., Janson, L., and Lv, J. (2018). Panning for gold:‘model-x’knockoffs for high dimensional controlled variable selection. Journal of the Royal Statistical Society: Series B (Statistical Methodology) , 80(3):551--577

  9. [17]

    Chang, T., Ko, D., Royer, J.-Y., and Lu, J. (2000). Regression techniques in plate tectonics. Statistical Science , pages 342--356

  10. [18]

    and Li, H

    Chen, J. and Li, H. (2013). Variable selection for sparse dirichlet-multinomial regression with an application to microbiome data analysis. The annals of applied statistics , 7(1)

  11. [19]

    Chernozhukov, V., Chetverikov, D., Demirer, M., Duflo, E., Hansen, C., Newey, W., and Robins, J. (2018). Double/debiased machine learning for treatment and structural parameters

  12. [20]

    and Voss, D

    Dean, A. and Voss, D. (1999). Design and analysis of experiments . Springer

  13. [21]

    and Schmidt, F

    Dodelson, S. and Schmidt, F. (2020). Modern cosmology . Academic press

  14. [22]

    Doran, G., Muandet, K., Zhang, K., and Sch \"o lkopf, B. (2014). A permutation-based kernel conditional independence test. In UAI , pages 132--141

  15. [23]

    A., Hron, K., and Olds, T

    Dumuid, D., Pedi s i \'c , Z ., Palarea-Albaladejo, J., Mart \' n-Fern \'a ndez, J. A., Hron, K., and Olds, T. (2020). Compositional data analysis in time-use epidemiology: what, why, how. International journal of environmental research and public health , 17(7):2220

  16. [24]

    Edwards, D. (2012). Introduction to graphical modelling . Springer Science & Business Media

  17. [25]

    J., Pawlowsky-Glahn, V., Mateu-Figueras, G., and Barcelo-Vidal, C

    Egozcue, J. J., Pawlowsky-Glahn, V., Mateu-Figueras, G., and Barcelo-Vidal, C. (2003). Isometric logratio transformations for compositional data analysis. Mathematical geology , 35(3):279--300

  18. [26]

    completely randomised

    Festing, M. F. (2020). The “completely randomised” and the “randomised block” are the only experimental designs suitable for widespread use in pre-clinical research. Scientific reports , 10(1):17577

  19. [27]

    Fiksel, J., Zeger, S., and Datta, A. (2022). A transformation-free linear regression for compositional outcomes and predictors. Biometrics , 78(3):974--987

  20. [28]

    and Hron, K

    Filzmoser, P. and Hron, K. (2009). Correlation analysis for compositional data. Mathematical Geosciences , 41:905--919

  21. [29]

    Filzmoser, P., Hron, K., and Reimann, C. (2009). Principal component analysis for compositional data with outliers. Environmetrics: The Official Journal of the International Environmetrics Society , 20(6):621--632

  22. [30]

    Filzmoser, P., Hron, K., Templ, M., Filzmoser, P., Hron, K., and Templ, M. (2018). Methods for high-dimensional compositional data. Applied Compositional Data Analysis: With Worked Examples in R , pages 207--225

  23. [31]

    Freeden, W., Gervens, T., and Schreiner, M. (1998). Constructive approximation on the sphere: with applications to geomathematics . Oxford University Press

  24. [32]

    J., Holmes, A

    Friston, K. J., Holmes, A. P., Price, C., B \"u chel, C., and Worsley, K. (1999). Multisubject fmri studies and conjunction analyses. Neuroimage , 10(4):385--396

  25. [33]

    B., Macklaim, J

    Gloor, G. B., Macklaim, J. M., Pawlowsky-Glahn, V., and Egozcue, J. J. (2017). Microbiome datasets are compositional: and this is not optional. Frontiers in microbiology , 8:2224

  26. [34]

    Green, P. E. and Srinivasan, V. (1978). Conjoint analysis in consumer research: issues and outlook. Journal of consumer research , 5(2):103--123

  27. [35]

    Greenacre, M., Mart \' nez- \'A lvaro, M., and Blasco, A. (2021). Compositional data analysis of microbiome and any-omics datasets: a validation of the additive logratio transformation. Frontiers in microbiology , 12:727398

  28. [36]

    and Southgate, D

    Greenfield, H. and Southgate, D. A. (2003). Food composition data: production, management, and use . Food & Agriculture Org

  29. [37]

    and Yekutieli, D

    Heller, R. and Yekutieli, D. (2014). Replicability analysis for genome-wide association studies. The Annals of Applied Statistics , 8(1):481--498

  30. [38]

    Holm, S. (1979). A simple sequentially rejective multiple test procedure. Scandinavian journal of statistics , pages 65--70

  31. [39]

    and Javadi, H

    Javanmard, A. and Javadi, H. (2019). False discovery rate control via debiased lasso . Electronic Journal of Statistics , 13(1):1212 -- 1253

  32. [40]

    and Montanari, A

    Javanmard, A. and Montanari, A. (2018). Debiasing the lasso: Optimal sample size for gaussian designs

  33. [41]

    and Coenders, G

    Joueid, A. and Coenders, G. (2018). Marketing innovation and new product portfolios. a compositional approach. Journal of Open Innovation: Technology, Market, and Complexity , 4(2):19

  34. [42]

    Kim, I., Neykov, M., Balakrishnan, S., and Wasserman, L. (2022). Local permutation tests for conditional independence. The Annals of Statistics , 50(6):3388--3414

  35. [43]

    K., Kolassa, J

    Kuchibhotla, A. K., Kolassa, J. E., and Kuffner, T. A. (2022). Post-selection inferenced. Annual Review of Statistics and Its Application , 9:505--527

  36. [44]

    and Peddada, S

    Lin, H. and Peddada, S. D. (2024). Multigroup analysis of compositions of microbiomes with covariate adjustments and repeated measures. Nature Methods , 21(1):83--91

  37. [45]

    Lin, S.-B. (2019). Nonparametric regression using needlet kernels for spherical data. Journal of Complexity , 50:66--83

  38. [46]

    Lin, W., Shi, P., Feng, R., and Li, H. (2014). Variable selection in regression with compositional covariates. Biometrika , 101(4):785--797

  39. [47]

    Liu, M., Katsevich, E., Janson, L., and Ramdas, A. (2022). Fast and powerful conditional randomization testing via distillation. Biometrika , 109(2):277--293

  40. [48]

    Lu, J., Shi, P., and Li, H. (2019). Generalized linear models with linear constraints for microbiome compositional data. Biometrics , 75(1):235--244

  41. [49]

    R., Kim, I., Shah, R

    Lundborg, A. R., Kim, I., Shah, R. D., and Samworth, R. J. (2022). The projected covariance measure for assumption-lean variable significance testing. arXiv preprint arXiv:2211.02039

  42. [50]

    Ma, S., Huttenhower, C., and Janson, L. (2024). Compositional differential abundance testing: Defining and finding a new type of health-microbiome associations. bioRxiv

  43. [51]

    J., Ma, S., Zhang, Y., Nguyen, L

    Mallick, H., Rahnavard, A., McIver, L. J., Ma, S., Zhang, Y., Nguyen, L. H., Tickle, T. L., Weingart, G., Ren, B., Schwager, E. H., et al. (2021). Multivariable association discovery in population-scale meta-omics studies. PLoS computational biology , 17(11):e1009442

  44. [52]

    Minka, T. (2000). Estimating a dirichlet distribution

  45. [53]

    Montgomery, D. C. (2017). Design and analysis of experiments . John wiley & sons

  46. [54]

    C., Peck, E

    Montgomery, D. C., Peck, E. A., and Vining, G. G. (2021). Introduction to linear regression analysis . John Wiley & Sons

  47. [55]

    N., Carpov, D., Chapados, N., and Bengio, Y

    Oreshkin, B. N., Carpov, D., Chapados, N., and Bengio, Y. (2019). N-beats: Neural basis expansion analysis for interpretable time series forecasting. arXiv preprint arXiv:1905.10437

  48. [56]

    Owen, A. B. (2009). Karl pearson’s meta-analysis revisited

  49. [57]

    and Heumann, C

    Pal, S. and Heumann, C. (2022). Clustering compositional data using dirichlet mixture model. Plos one , 17(5):e0268438

  50. [58]

    N., Stine, O

    Paulson, J. N., Stine, O. C., Bravo, H. C., and Pop, M. (2013). Differential abundance analysis for microbial marker-gene surveys. Nature methods , 10(12):1200--1202

  51. [59]

    and Buccianti, A

    Pawlowsky-Glahn, V. and Buccianti, A. (2011). Compositional data analysis . Wiley Online Library

  52. [60]

    Pearl, J. (1988). Chapter 3 - markov and bayesian networks: Two graphical representations of probabilistic knowledge. In Pearl, J., editor, Probabilistic Reasoning in Intelligent Systems , pages 77--141. Morgan Kaufmann, San Francisco (CA)

  53. [61]

    Z., Suram, S

    Pesenson, M. Z., Suram, S. K., and Gregoire, J. M. (2015). Statistical analysis and interpolation of compositional data in materials science. ACS combinatorial science , 17(2):130--136

  54. [62]

    Peters, J. (2015). On the intersection property of conditional independence and its application to causal discovery. Journal of Causal Inference , 3(1):97--108

  55. [63]

    J., Pawlowsky-Glahn, V., Paredes, R., Noguera-Julian, M., and Calle, M

    Rivera-Pinto, J., Egozcue, J. J., Pawlowsky-Glahn, V., Paredes, R., Noguera-Julian, M., and Calle, M. L. (2018). Balances: a new perspective for microbiome analysis. MSystems , 3(4):10--1128

  56. [64]

    Rodrigues, P. C. and Lima, A. T. (2009). Analysis of an european union election using principal component analysis. Statistical Papers , 50:895--904

  57. [65]

    Schwarz, G. (1978). Estimating the dimension of a model. The annals of statistics , pages 461--464

  58. [66]

    T., Shanmugam, K., Dimakis, A

    Sen, R., Suresh, A. T., Shanmugam, K., Dimakis, A. G., and Shakkottai, S. (2017). Model-powered conditional independence test. Advances in neural information processing systems , 30

  59. [67]

    Shah, R. D. and Peters, J. (2020). The hardness of conditional independence testing and the generalised covariance measure. The Annals of Statistics , 48(3)

  60. [68]

    Shi, H., Drton, M., and Han, F. (2024). On azadkia--chatterjee’s conditional dependence coefficient. Bernoulli , 30(2):851--877

  61. [69]

    Shi, P., Zhang, A., and Li, H. (2016). Regression analysis for microbiome compositional data. The Annals of Applied Statistics

  62. [70]

    Simes, R. J. (1986). An improved bonferroni procedure for multiple tests of significance. Biometrika , 73(3):751--754

  63. [71]

    Sohn, M. B. and Li, H. (2019). Compositional mediation analysis for microbiome studies. The Annals of Applied Statistics , 13(1):661--681

  64. [72]

    Srinivasan, A., Xue, L., and Zhan, X. (2021). Compositional knockoff filter for high-dimensional regression analysis of microbiome data. Biometrics , 77(3):984--995

  65. [73]

    and John, P

    Stoker, G. and John, P. (2009). Design experiments: Engaging policy makers in the search for evidence about what works. Political Studies , 57(2):356--373

  66. [74]

    Tansey, W., Veitch, V., Zhang, H., Rabadan, R., and Blei, D. M. (2022). The holdout randomization test for feature selection in black box models. Journal of Computational and Graphical Statistics , 31(1):151--162

  67. [75]

    Tibshirani, R. (1996). Regression shrinkage and selection via the lasso. Journal of the Royal Statistical Society Series B: Statistical Methodology , 58(1):267--288

  68. [76]

    J., Ley, R

    Turnbaugh, P. J., Ley, R. E., Hamady, M., Fraser-Liggett, C. M., Knight, R., and Gordon, J. I. (2007). The human microbiome project. Nature , 449(7164):804--810

  69. [77]

    M., Ewald, A

    Tyszka, J. M., Ewald, A. J., Wallingford, J. B., and Fraser, S. E. (2005). New tools for visualization and analysis of morphogenesis in spherical embryos. Developmental dynamics: an official publication of the American Association of Anatomists , 234(4):974--983

  70. [78]

    J., Sabatti, C., and Owen, A

    Wang, J., Gui, L., Su, W. J., Sabatti, C., and Owen, A. B. (2016). Detecting multiple replicating signals using adaptive filtering procedures. arXiv preprint arXiv:1610.03330

  71. [79]

    and Owen, A

    Wang, J. and Owen, A. B. (2019). Admissibility in partial conjunction testing. Journal of the American Statistical Association , 114(525):158--168

  72. [80]

    and Fang, J.-Y

    Wang, N. and Fang, J.-Y. (2023). Fusobacterium nucleatum, a key pathogenic factor and microbial biomarker for colorectal cancer. Trends in Microbiology , 31(2):159--172

  73. [81]

    Wang, S. (2023). Robust differential abundance test in compositional data. Biometrika , 110(1):169--185

  74. [82]

    Wright, S. P. (1992). Adjusted p-values for simultaneous inference. Biometrics , pages 1005--1013

  75. [83]

    K., and Li, H

    Xia, F., Chen, J., Fung, W. K., and Li, H. (2013). A logistic normal multinomial regression model for microbiome compositional data analysis. Biometrics , 69(4):1053--1063

  76. [84]

    Xing, X., Zhao, Z., and Liu, J. S. (2023). Controlling false discovery rate using gaussian mirrors. Journal of the American Statistical Association , 118(541):222--241

  77. [85]

    and Benjamini, Y

    Yekutieli, D. and Benjamini, Y. (1999). Resampling-based false discovery rate controlling multiple test procedures for correlated test statistics. Journal of Statistical Planning and Inference , 82(1-2):171--196

  78. [86]

    Zhang, T. (2008). Adaptive forward-backward greedy algorithm for sparse learning with linear models. In Koller, D., Schuurmans, D., Bengio, Y., and Bottou, L., editors, Advances in Neural Information Processing Systems , volume 21. Curran Associates, Inc

  79. [87]

    Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., and Friedman, J. M. (1994). Positional cloning of the mouse obese gene and its human homologue. Nature , 372(6505):425--432

  80. [88]

    O'Reilly Media, Inc

    Zheng, A. and Casari, A. (2018). Feature engineering for machine learning: principles and techniques for data scientists . " O'Reilly Media, Inc."

  81. [89]

    Zhou, H., He, K., Chen, J., and Zhang, X. (2022). Linda: linear models for differential abundance analysis of microbiome compositional data. Genome biology , 23(1):1--23

  82. [90]

    Zong, Y., Zhao, H., and Wang, T. (2024). mbdecoda: a debiased approach to compositional data analysis for microbiome surveys. Briefings in Bioinformatics , 25(3):bbae205

Pith tools

Reviewed August 10, 2026 · model on record in the stance chip above.